priapism
Information
- Disease name
- priapism
- Disease ID
- DOID:9286
- Description
- "A peripheral vascular disease characterized by blood trapped in the penis that is unable to drain." [url:http\://en.wikipedia.org/wiki/Priapism, url:http\://my.clevelandclinic.org/disorders/priapism/hic_priapism.aspx]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes | Mutation | Description | Source | Links |
---|
NCT ID | Status | Phase | Summary | Start date | Completion date |
---|---|---|---|---|---|
NCT00300235 | Completed | Priapism in Boys and Men With Sickle Cell Disease - Demographics, Characteristics and Prevalence | August 2005 | March 2008 | |
NCT00940901 | Completed | Phase 2 | Sildenafil for Treatment of Priapism in Men With Sickle Cell Anemia | June 2008 | December 2013 |
NCT03938454 | Completed | Phase 2 | A Study to Evaluate the Safety and Efficacy of Crizanlizumab in Sickle Cell Disease Related Priapism | October 16, 2019 | November 29, 2023 |
NCT04932902 | Enrolling by invitation | ManAgement of pRiapiSm and Its Impact on Outcomes | June 1, 2021 | December 31, 2025 | |
NCT00538564 | Withdrawn | Phase 2 | Tadalafil for Treatment of Priapism in Men With Sickle Cell Anemia | November 2006 | August 2009 |
NCT01940718 | Withdrawn | Early Phase 1 | Androgen Regulation of Priapism in Sickle Cell Disease | March 2014 | January 2016 |
- Disase is a (Disease Ontology)
- DOID:341
- Cross Reference ID (Disease Ontology)
- GARD:10016
- Cross Reference ID (Disease Ontology)
- ICD10CM:N48.3
- Cross Reference ID (Disease Ontology)
- ICD9CM:607.3
- Cross Reference ID (Disease Ontology)
- MESH:D011317
- Cross Reference ID (Disease Ontology)
- NCI:C85022
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:155930001
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0033117
- Exact Synonym (Disease Ontology)
- Mentulagra
- HPO Human Phenotype ID (Human Phenotype Ontology)
- HP:0200023
- MedGen concept unique identifier (MedGen Concept name)
- C0033117
- MedGen concept unique identifier (MedGen Concept name)
- C1867771
- MedGen unique identifier (MedGen Concept name)
- 19462
- MedGen unique identifier (MedGen Concept name)
- 356846
- ICD10 preferred id (Insert disease from ICD10)
- D0011385
- ICD10 class code (Insert disease from ICD10)
- N48.3
- MeSH unique ID (MeSH (Medical Subject Headings))
- D011317